Your specialist in Quality and Compliance Management within Life Science.
The complex rules of our regulated industry are changing constantly. Your business needs to keep up with that change to be compliant, and deliver quality. Let us guide you.
Q-People provides targeted solutions in Quality and Compliance projects in the Life Sciences sector, from Pharmaceutical and Biotech to API and Medical Device Production.
What we do
Q-People helps companies to set up and support Quality and Compliance processes, procedures and systems. Training, mentoring and coaching of talent within the Life Sciences sector is our strength. We don’t want specialist knowledge or talent to go to waste.
Every quality process requires an approach tailored to the specific needs of the production environment. We map out the current situation in accordance with the latest legislation.
Through validation and controlling quality risks we guarantee that your company complies with regulations and product safety is guaranteed.
meet our satisfied customers
Domains of expertise
We offer support and knowledge in all domains of Quality and CGMP Compliance Management.
- Design and development of quality management systems
- Assistance in defining compliancy strategies
- Validation Processes, software and equipment
- Control of quality risks
- Preparation of quality and compliance audits
- Are educated and committed people who will bring added-value
- Have a background in the Life Sciences sector
- Are uniquely skilled, to cover the Full Quality Management System
- Will continuously be trained and certified
- Guarantee a powerful level of engagement
Meet our Q-Experts
Pharma 4.0: Redefining Product Development and Regulatory OperationsAligning with the industry requirements has always been a priority for organizations. En route, they are heavily relying on revolutions that can help them stay ahead of the competition. One such revolution is Industry 4.0 – an amalgamation of pathbreaking technologies like industrial internet of things (IIoT), big data, artificial intelligence (AI), etc. The industry 4.0 has automated and optimized companies’ business processes and business models.
Successful Technical Writing TrainingA successful training session "Technical Writing: Deviation Handling" at Darwin wetenschapspark, Niel. This in close collaboration with Co-valent (vormingsfonds PC 116 & 207). This training gives trainees a broad background in GMP Writing Skills. The aim of this course is to enhance the employees GMP writing skills in different areas to write clear, readable and defendable documents. The style and skills required for formal business writing are best developed by practice and experience, but with the right tools and know-how it is a first start. The aim of the training is to develop the ability to perform the tasks individually and right first time.
December 16 @ 8:30 am – December 17 @ 5:00 pm
December 18 @ 8:30 am
23rd March 2020 @ 8:30 am – 5:00 pm
27th April 2020 @ 8:30 am – 5:00 pm
29th May 2020 @ 8:30 am – 5:00 pm